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Measures / Standards
# Name Type Agency Description Law Valid To Apply To
1 Registration requirement for the import of medical products Registration Requirement Ministry of Health the import of medical products and health supplement products must be registered with the department of food and drug, ministry of health.
  1. Decision on business establishment on medicines and medical equipment (Revised Version) no.1820/MoH, dated 25 August 2017.
  2. Decision on the registration and verification of medical devices, No. 1470/MOH, dated 11 July 2023.
  3. Law on Drugs and Medical Products (Amendment) No.07/NA, Dated 10 March 2026
 9999-12-31 ALL
2 Requirement for Registration or Notification of Medical Product Exports Registration Requirement Ministry of Health Legal entities or organizations exporting medical products are required to register or notify the relevant authorities of the medical products by providing details such as the product name, ingredients or manufacturer’s formula, dosage form, strength, packaging unit, international code, and source of the medical products. This is to ensure that business operations are conducted properly and in compliance with established legislation, as well as regional and international standards, while also ensuring product quality and consumer safety.
  1. Decision on the registration and verification of medical devices, No. 1470/MOH, dated 11 July 2023.
  2. Law on Drugs and Medical Products (Amendment) No.07/NA, Dated 10 March 2026
 (not set) ALL
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